|
JP4145955B2
(en)
*
|
1994-09-29 |
2008-09-03 |
ノバルティス アクチェンゲゼルシャフト |
Pyrrolo [2,3-d] pyrimidine and use thereof
|
|
TW321649B
(en)
*
|
1994-11-12 |
1997-12-01 |
Zeneca Ltd |
|
|
GB9424233D0
(en)
*
|
1994-11-30 |
1995-01-18 |
Zeneca Ltd |
Quinazoline derivatives
|
|
JP4249804B2
(en)
*
|
1995-04-03 |
2009-04-08 |
ノバルティス・アクチエンゲゼルシャフト |
Pyrazole derivative and process for producing the same
|
|
EP0824525B1
(en)
*
|
1995-04-27 |
2001-06-13 |
AstraZeneca AB |
Quinazoline derivatives
|
|
GB9508535D0
(en)
*
|
1995-04-27 |
1995-06-14 |
Zeneca Ltd |
Quinazoline derivative
|
|
GB9508537D0
(en)
*
|
1995-04-27 |
1995-06-14 |
Zeneca Ltd |
Quinazoline derivatives
|
|
GB9508565D0
(en)
*
|
1995-04-27 |
1995-06-14 |
Zeneca Ltd |
Quiazoline derivative
|
|
GB9508538D0
(en)
*
|
1995-04-27 |
1995-06-14 |
Zeneca Ltd |
Quinazoline derivatives
|
|
US6395733B1
(en)
*
|
1995-06-07 |
2002-05-28 |
Pfizer Inc |
Heterocyclic ring-fused pyrimidine derivatives
|
|
EP0836605B1
(en)
*
|
1995-07-06 |
2002-02-06 |
Novartis AG |
Pyrrolopyrimidines and processes for the preparation thereof
|
|
GB9624482D0
(en)
|
1995-12-18 |
1997-01-15 |
Zeneca Phaema S A |
Chemical compounds
|
|
AU1441497A
(en)
*
|
1996-01-23 |
1997-08-20 |
Novartis Ag |
Pyrrolopyrimidines and processes for their preparation
|
|
CH690773A5
(en)
*
|
1996-02-01 |
2001-01-15 |
Novartis Ag |
Pyrrolo (2,3-d) pyrimides and their use.
|
|
US5760041A
(en)
*
|
1996-02-05 |
1998-06-02 |
American Cyanamid Company |
4-aminoquinazoline EGFR Inhibitors
|
|
WO1997030035A1
(en)
|
1996-02-13 |
1997-08-21 |
Zeneca Limited |
Quinazoline derivatives as vegf inhibitors
|
|
GB9603095D0
(en)
*
|
1996-02-14 |
1996-04-10 |
Zeneca Ltd |
Quinazoline derivatives
|
|
GB9603097D0
(en)
*
|
1996-02-14 |
1996-04-10 |
Zeneca Ltd |
Quinazoline compounds
|
|
GB9604361D0
(en)
*
|
1996-02-29 |
1996-05-01 |
Pharmacia Spa |
4-Substituted pyrrolopyrimidine compounds as tyrosine kinase inhibitors
|
|
ES2169355T3
(en)
|
1996-03-05 |
2002-07-01 |
Astrazeneca Ab |
DERIVATIVES OF 4-ANILINOQUINAZOLINA.
|
|
JP3370340B2
(en)
|
1996-04-12 |
2003-01-27 |
ワーナー―ランバート・コンパニー |
Irreversible inhibitors of tyrosine kinase
|
|
GB9607729D0
(en)
*
|
1996-04-13 |
1996-06-19 |
Zeneca Ltd |
Quinazoline derivatives
|
|
AU720429B2
(en)
*
|
1996-08-23 |
2000-06-01 |
Novartis Ag |
Substituted pyrrolopyrimidines and processes for their preparation
|
|
ES2239779T3
(en)
|
1996-10-02 |
2005-10-01 |
Novartis Ag |
PIRIMIDINE DERIVATIVES AND PROCEDURES FOR THE PREPARATION OF THE SAME.
|
|
DE69728688T2
(en)
|
1996-11-19 |
2004-08-19 |
Amgen Inc., Thousand Oaks |
ARYL AND HETEROARYL SUBSTITUTED CONDENSED PYRROLE AS AN ANTI-FLAMMING AGENT
|
|
CA2272705C
(en)
*
|
1996-11-27 |
2003-03-18 |
Pfizer Inc. |
Fused bicyclic pyrimidine derivatives
|
|
US7863444B2
(en)
|
1997-03-19 |
2011-01-04 |
Abbott Laboratories |
4-aminopyrrolopyrimidines as kinase inhibitors
|
|
US6002008A
(en)
*
|
1997-04-03 |
1999-12-14 |
American Cyanamid Company |
Substituted 3-cyano quinolines
|
|
US5929080A
(en)
*
|
1997-05-06 |
1999-07-27 |
American Cyanamid Company |
Method of treating polycystic kidney disease
|
|
US6251912B1
(en)
|
1997-08-01 |
2001-06-26 |
American Cyanamid Company |
Substituted quinazoline derivatives
|
|
IL133430A0
(en)
*
|
1997-08-05 |
2001-04-30 |
Pfizer Prod Inc |
4-AMINOPYRROLE (3, 2-d) PYRIMIDINES AS NEUROPEPTIDE Y RECEPTOR ANTAGONISTS
|
|
US6323209B1
(en)
|
1997-11-06 |
2001-11-27 |
American Cyanamid Company |
Method of treating or inhibiting colonic polyps
|
|
US6187777B1
(en)
*
|
1998-02-06 |
2001-02-13 |
Amgen Inc. |
Compounds and methods which modulate feeding behavior and related diseases
|
|
AU3053999A
(en)
|
1998-03-31 |
1999-10-25 |
Kyowa Hakko Kogyo Co. Ltd. |
Nitrogenous heterocyclic compounds
|
|
US6878716B1
(en)
|
1998-06-02 |
2005-04-12 |
Osi Pharmaceuticals, Inc. |
Compounds specific to adenosine A1 receptor and uses thereof
|
|
IL139787A0
(en)
*
|
1998-06-02 |
2002-02-10 |
Osi Pharm Inc |
PYRROLO [2, 3d] PYRIMIDINE COMPOSITIONS AND THEIR USE
|
|
US6686366B1
(en)
|
1998-06-02 |
2004-02-03 |
Osi Pharmaceuticals, Inc. |
Compounds specific to adenosine A3 receptor and uses thereof
|
|
PL198640B1
(en)
|
1998-06-19 |
2008-07-31 |
Pfizer Prod Inc |
PYRROLO[2,3-d]PYRIMIDINE COMPOUNDS
|
|
PA8474101A1
(en)
|
1998-06-19 |
2000-09-29 |
Pfizer Prod Inc |
PYROLEUM [2,3-D] PIRIMIDINE COMPOUNDS
|
|
HK1039325B
(en)
*
|
1998-09-18 |
2006-02-24 |
Abbott Gmbh & Co. Kg |
4-aminopyrrolopyrimidines as kinase inhibitors
|
|
US6713474B2
(en)
|
1998-09-18 |
2004-03-30 |
Abbott Gmbh & Co. Kg |
Pyrrolopyrimidines as therapeutic agents
|
|
US6288082B1
(en)
|
1998-09-29 |
2001-09-11 |
American Cyanamid Company |
Substituted 3-cyanoquinolines
|
|
US6297258B1
(en)
|
1998-09-29 |
2001-10-02 |
American Cyanamid Company |
Substituted 3-cyanoquinolines
|
|
AU6159499A
(en)
|
1998-09-29 |
2000-04-17 |
Wyeth Holdings Corporation |
Substituted 3-cyanoquinolines as protein tyrosine kinases inhibitors
|
|
EP1669071B1
(en)
*
|
1999-05-21 |
2009-07-22 |
Bristol-Myers Squibb Company |
Pyrrolotriazine inhibitors of kinases
|
|
US6982265B1
(en)
|
1999-05-21 |
2006-01-03 |
Bristol Myers Squibb Company |
Pyrrolotriazine inhibitors of kinases
|
|
CZ303660B6
(en)
*
|
1999-05-21 |
2013-02-13 |
Bristol-Myers Squibb Company |
Pyrrolotriazines and pharmaceutical composition containing thereof
|
|
US6432979B1
(en)
|
1999-08-12 |
2002-08-13 |
American Cyanamid Company |
Method of treating or inhibiting colonic polyps and colorectal cancer
|
|
US7071199B1
(en)
|
1999-09-17 |
2006-07-04 |
Abbott Gmbh & Cco. Kg |
Kinase inhibitors as therapeutic agents
|
|
CN100376567C
(en)
|
1999-11-05 |
2008-03-26 |
阿斯特拉曾尼卡有限公司 |
Quinazoline derivatives as VEGF inhibitors
|
|
US7160890B2
(en)
|
1999-12-02 |
2007-01-09 |
Osi Pharmaceuticals, Inc. |
Compounds specific to adenosine A3 receptor and uses thereof
|
|
US6664252B2
(en)
|
1999-12-02 |
2003-12-16 |
Osi Pharmaceuticals, Inc. |
4-aminopyrrolo[2,3-d]pyrimidine compounds specific to adenosine A2a receptor and uses thereof
|
|
US6680322B2
(en)
|
1999-12-02 |
2004-01-20 |
Osi Pharmaceuticals, Inc. |
Compounds specific to adenosine A1 receptors and uses thereof
|
|
EA006227B1
(en)
|
1999-12-10 |
2005-10-27 |
Пфайзер Продактс Инк. |
PIRROLO(2,3-d)PYRIMIDINE COMPOUNDS
|
|
EA006153B1
(en)
|
2000-06-26 |
2005-10-27 |
Пфайзер Продактс Инк. |
PYRROLO[2,3-d]PYRIMIDINE COMPOUNDS AS IMMUNOSUPPRESSIVE AGENTS
|
|
US6503914B1
(en)
*
|
2000-10-23 |
2003-01-07 |
Board Of Regents, The University Of Texas System |
Thienopyrimidine-based inhibitors of the Src family
|
|
US6867300B2
(en)
*
|
2000-11-17 |
2005-03-15 |
Bristol-Myers Squibb Company |
Methods for the preparation of pyrrolotriazine compounds useful as kinase inhibitors
|
|
US6670357B2
(en)
*
|
2000-11-17 |
2003-12-30 |
Bristol-Myers Squibb Company |
Methods of treating p38 kinase-associated conditions and pyrrolotriazine compounds useful as kinase inhibitors
|
|
US6680324B2
(en)
|
2000-12-01 |
2004-01-20 |
Osi Pharmaceuticals, Inc. |
Compounds specific to adenosine A1 receptors and uses thereof
|
|
US6673802B2
(en)
|
2000-12-01 |
2004-01-06 |
Osi Pharmaceuticals, Inc. |
Compounds specific to adenosine A3 receptor and uses thereof
|
|
ES2259707T3
(en)
*
|
2001-05-14 |
2006-10-16 |
Novartis Ag |
OXAZOLO AND FUROPIRIMIDINAS AND ITS USE IN DRUGS MEDICINES.
|
|
US7301023B2
(en)
|
2001-05-31 |
2007-11-27 |
Pfizer Inc. |
Chiral salt resolution
|
|
US7323469B2
(en)
|
2001-08-07 |
2008-01-29 |
Novartis Ag |
7H-pyrrolo[2,3-d]pyrimidine derivatives
|
|
GB0119249D0
(en)
|
2001-08-07 |
2001-10-03 |
Novartis Ag |
Organic compounds
|
|
CN1523991A
(en)
*
|
2001-08-10 |
2004-08-25 |
��˹��ŵ�� |
Use of a c-Src inhibitor alone or in combination with STI571 for the treatment of leukemia
|
|
GB0121033D0
(en)
*
|
2001-08-30 |
2001-10-24 |
Novartis Ag |
Organic compounds
|
|
US6770652B2
(en)
*
|
2001-10-18 |
2004-08-03 |
Duquesne University Of The Holy Ghost |
Multiple acting anti-angiogenic and cytotoxic compounds and methods for using the same
|
|
DE60234118D1
(en)
|
2001-11-30 |
2009-12-03 |
Osi Pharm Inc |
Compounds specific for adenosine A1 and A3 receptors and their applications
|
|
PY0228255A
(en)
*
|
2001-12-06 |
2004-06-01 |
Pfizer Prod Inc |
NOVEL CRYSTALLINE COMPOUNDS
|
|
US20030229067A1
(en)
|
2001-12-20 |
2003-12-11 |
Arlindo Castelhano |
Pyrrolopyrimidine A2b selective antagonist compounds, their synthesis and use
|
|
BR0215202A
(en)
|
2001-12-20 |
2004-10-13 |
Osi Pharm Inc |
A2b selective pyrimidine antagonist compounds, their synthesis and use
|
|
US6805491B2
(en)
*
|
2002-05-20 |
2004-10-19 |
Stratos International, Inc. |
Stub having an optical fiber
|
|
EP1534715B1
(en)
*
|
2002-07-11 |
2007-08-15 |
Bayer Pharmaceuticals Corporation |
Furopyridine and furopyrimidine derivatives for the treatment of hyper-proliferative disorders
|
|
AU2003276591A1
(en)
|
2002-11-26 |
2004-06-18 |
Pfizer Products Inc. |
Method of treatment of transplant rejection
|
|
US7253166B2
(en)
|
2003-04-22 |
2007-08-07 |
Irm Llc |
6-phenyl-7H-pyrrolo[2,3-d]pyrimidine compounds that induce neuronal differentiation in embryonic stem cells
|
|
CA2530281C
(en)
*
|
2003-07-24 |
2013-02-12 |
Bayer Pharmaceuticals Corporation |
Substituted tetrahydrobenzothienopyrimidinamine compounds useful for treating hyper-proliferative disorders
|
|
GB0317663D0
(en)
*
|
2003-07-29 |
2003-09-03 |
Astrazeneca Ab |
Pharmaceutical composition
|
|
US20050187389A1
(en)
*
|
2004-01-13 |
2005-08-25 |
Ambit Biosciences Corporation |
Pyrrolopyrimidine derivatives and analogs and their use in the treatment and prevention of diseases
|
|
US20070197559A1
(en)
*
|
2004-03-02 |
2007-08-23 |
Rajagopal Bakthavatchalam |
Aryl substituted purine analogues
|
|
HRP20090495T1
(en)
*
|
2004-04-02 |
2009-10-31 |
Osi Pharmaceuticals |
6,6-bicyclic ring substituted heterobicyclic protein kinase inhibitors
|
|
US7439246B2
(en)
*
|
2004-06-28 |
2008-10-21 |
Bristol-Myers Squibb Company |
Fused heterocyclic kinase inhibitors
|
|
US7504521B2
(en)
*
|
2004-08-05 |
2009-03-17 |
Bristol-Myers Squibb Co. |
Methods for the preparation of pyrrolotriazine compounds
|
|
TW200618803A
(en)
|
2004-08-12 |
2006-06-16 |
Bristol Myers Squibb Co |
Process for preparing pyrrolotriazine aniline compounds useful as kinase inhibitors
|
|
EP1899353A1
(en)
*
|
2005-06-22 |
2008-03-19 |
DeveloGen Aktiengesellschaft |
Thienopyrimidines for pharmaceutical compositions
|
|
JP5302883B2
(en)
|
2006-04-07 |
2013-10-02 |
ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング |
Thienopyrimidine having MNK1 / MNK2 inhibitory activity for pharmaceutical composition
|
|
EP1889847A1
(en)
*
|
2006-07-10 |
2008-02-20 |
DeveloGen Aktiengesellschaft |
Pyrrolopyrimidines for pharmaceutical compositions
|
|
HRP20140395T1
(en)
|
2008-08-20 |
2014-06-06 |
Zoetis Llc |
PIROLO [2,3-d] PIRIMIDINE COMPOUNDS
|
|
KR20110045019A
(en)
|
2008-08-26 |
2011-05-03 |
베링거 인겔하임 인터내셔날 게엠베하 |
Thienopyrimidine for Pharmaceutical Compositions
|
|
US8385364B2
(en)
*
|
2008-09-24 |
2013-02-26 |
Nec Laboratories America, Inc. |
Distributed message-passing based resource allocation in wireless systems
|
|
PE20100362A1
(en)
|
2008-10-30 |
2010-05-27 |
Irm Llc |
PURINE DERIVATIVES THAT EXPAND HEMATOPOYETIC STEM CELLS
|
|
WO2010054264A1
(en)
|
2008-11-07 |
2010-05-14 |
Triact Therapeutics, Inc. |
Use of catecholic butane derivatives in cancer therapy
|
|
WO2010099139A2
(en)
|
2009-02-25 |
2010-09-02 |
Osi Pharmaceuticals, Inc. |
Combination anti-cancer therapy
|
|
WO2010099137A2
(en)
|
2009-02-26 |
2010-09-02 |
Osi Pharmaceuticals, Inc. |
In situ methods for monitoring the emt status of tumor cells in vivo
|
|
US8465912B2
(en)
|
2009-02-27 |
2013-06-18 |
OSI Pharmaceuticals, LLC |
Methods for the identification of agents that inhibit mesenchymal-like tumor cells or their formation
|
|
WO2010099138A2
(en)
|
2009-02-27 |
2010-09-02 |
Osi Pharmaceuticals, Inc. |
Methods for the identification of agents that inhibit mesenchymal-like tumor cells or their formation
|
|
US8642834B2
(en)
|
2009-02-27 |
2014-02-04 |
OSI Pharmaceuticals, LLC |
Methods for the identification of agents that inhibit mesenchymal-like tumor cells or their formation
|
|
US20120064072A1
(en)
|
2009-03-18 |
2012-03-15 |
Maryland Franklin |
Combination Cancer Therapy Comprising Administration of an EGFR Inhibitor and an IGF-1R Inhibitor
|
|
EP2510110A1
(en)
|
2009-11-13 |
2012-10-17 |
Pangaea Biotech S.L. |
Molecular biomarkers for predicting response to tyrosine kinase inhibitors in lung cancer
|
|
EA201201191A1
(en)
|
2010-02-26 |
2013-04-30 |
Бёрингер Ингельхайм Интернациональ Гмбх |
4- [CYCLOALKYLOXY (HETERO) ARYLAMINO] THIENO [2,3-D] PYRIMIDINES THAT HAVE INHIBITING ACTIVITY WITH RESPECT TO MNKL / MNK2 INTENDED FOR PHARMACEUTICAL COMPOSITIONS
|
|
UY33241A
(en)
|
2010-02-26 |
2011-09-30 |
Boehringer Ingelheim Int |
? Tienopyrimidines containing heterocycloalkyl for pharmaceutical compositions ?.
|
|
AR080328A1
(en)
|
2010-02-26 |
2012-03-28 |
Boehringer Ingelheim Int |
TIENOPIRIMIDINES CONTAINING A SUBSTITUTED RENTING GROUP, INHIBITORS OF MNK1 AND / OR MNK2 QUINASES, PHARMACEUTICAL COMPOSITIONS CONTAINING THEM AND USE OF THE SAME FOR THE TREATMENT OF METABOLIC DISORDERS SUCH AS DIABETES AND OTHERS
|
|
EP2468883A1
(en)
|
2010-12-22 |
2012-06-27 |
Pangaea Biotech S.L. |
Molecular biomarkers for predicting response to tyrosine kinase inhibitors in lung cancer
|
|
US9134297B2
(en)
|
2011-01-11 |
2015-09-15 |
Icahn School Of Medicine At Mount Sinai |
Method and compositions for treating cancer and related methods
|
|
EP2492688A1
(en)
|
2011-02-23 |
2012-08-29 |
Pangaea Biotech, S.A. |
Molecular biomarkers for predicting response to antitumor treatment in lung cancer
|
|
WO2012129145A1
(en)
|
2011-03-18 |
2012-09-27 |
OSI Pharmaceuticals, LLC |
Nscle combination therapy
|
|
CA2760174A1
(en)
*
|
2011-12-01 |
2013-06-01 |
Pharmascience Inc. |
Protein kinase inhibitors and uses thereof
|
|
CA2831843A1
(en)
*
|
2011-04-04 |
2012-10-11 |
Pharmascience Inc. |
Protein kinase inhibitors
|
|
JP2014519813A
(en)
|
2011-04-25 |
2014-08-21 |
オーエスアイ・ファーマシューティカルズ,エルエルシー |
Use of EMT gene signatures in cancer drug discovery, diagnosis, and treatment
|
|
CA2845179A1
(en)
|
2011-08-31 |
2013-03-07 |
Genentech, Inc. |
Diagnostic markers
|
|
WO2013055530A1
(en)
|
2011-09-30 |
2013-04-18 |
Genentech, Inc. |
Diagnostic methylation markers of epithelial or mesenchymal phenotype and response to egfr kinase inhibitor in tumours or tumour cells
|
|
WO2013152252A1
(en)
|
2012-04-06 |
2013-10-10 |
OSI Pharmaceuticals, LLC |
Combination anti-cancer therapy
|
|
JP2015518842A
(en)
*
|
2012-05-21 |
2015-07-06 |
バイエル ファーマ アクチエンゲゼルシャフト |
Substituted pyrrolopyrimidine
|
|
WO2013190089A1
(en)
|
2012-06-21 |
2013-12-27 |
Pangaea Biotech, S.L. |
Molecular biomarkers for predicting outcome in lung cancer
|
|
MD20140130A2
(en)
|
2012-06-29 |
2015-04-30 |
Pfizer Inc. |
Novel 4-(substituted-amino)-7H-pyrrolo[2,3-d]pyrimidines as LRRK2 inhibitors
|
|
EP2961412A4
(en)
|
2013-02-26 |
2016-11-09 |
Triact Therapeutics Inc |
Cancer therapy
|
|
WO2014145576A2
(en)
|
2013-03-15 |
2014-09-18 |
Northwestern University |
Substituted pyrrolo(2,3-d)pyrimidines for the treatment of cancer
|
|
EP2976085A1
(en)
|
2013-03-21 |
2016-01-27 |
INSERM - Institut National de la Santé et de la Recherche Médicale |
Method and pharmaceutical composition for use in the treatment of chronic liver diseases associated with a low hepcidin expression
|
|
US9381246B2
(en)
|
2013-09-09 |
2016-07-05 |
Triact Therapeutics, Inc. |
Cancer therapy
|
|
WO2015092592A1
(en)
|
2013-12-17 |
2015-06-25 |
Pfizer Inc. |
Novel 3,4-disubstituted-1h-pyrrolo[2,3-b]pyridines and 4,5-disubstituted-7h-pyrrolo[2,3-c]pyridazines as lrrk2 inhibitors
|
|
US20170027940A1
(en)
|
2014-04-10 |
2017-02-02 |
Stichting Het Nederlands Kanker Instituut |
Method for treating cancer
|
|
EP3237638B1
(en)
|
2014-12-24 |
2020-01-15 |
F.Hoffmann-La Roche Ag |
Therapeutic, diagnostic and prognostic methods for cancer of the bladder
|
|
CN108137586B
(en)
|
2015-09-14 |
2021-04-13 |
辉瑞大药厂 |
Novel imidazo[4,5-c]quinoline and imidazo[4,5-c][1,5]naphthyridine derivatives as LRRK2 inhibitors
|
|
CA3048217A1
(en)
|
2016-12-22 |
2018-06-28 |
Amgen Inc. |
Kras g12c inhibitors and methods of using the same
|
|
ES2905676T3
(en)
|
2017-05-22 |
2022-04-11 |
Amgen Inc |
KRAS G12C inhibitors and methods for their use
|
|
CN111051306B
(en)
|
2017-09-08 |
2023-01-03 |
美国安进公司 |
Inhibitors of KRAS G12C and methods of use thereof
|
|
ES2995514T3
(en)
|
2018-05-04 |
2025-02-10 |
Amgen Inc |
Kras g12c inhibitors and methods of using the same
|
|
MX2020010836A
(en)
|
2018-05-04 |
2021-01-08 |
Amgen Inc |
Kras g12c inhibitors and methods of using the same.
|
|
EP3790886B1
(en)
|
2018-05-10 |
2024-06-26 |
Amgen Inc. |
Kras g12c inhibitors for the treatment of cancer
|
|
US12115161B2
(en)
|
2018-05-11 |
2024-10-15 |
Keio University |
Prophylactic and/or therapeutic agent for inflammatory diseases which contains pyrrolopyrimidine compound as active ingredient
|
|
AU2019278998B2
(en)
|
2018-06-01 |
2023-11-09 |
Amgen Inc. |
KRAS G12C inhibitors and methods of using the same
|
|
MX2020012204A
(en)
|
2018-06-11 |
2021-03-31 |
Amgen Inc |
KRAS G12C INHIBITORS TO TREAT CANCER.
|
|
CA3100390A1
(en)
|
2018-06-12 |
2020-03-12 |
Amgen Inc. |
Kras g12c inhibitors encompassing piperazine ring and use thereof in the treatment of cancer
|
|
CA3115038A1
(en)
|
2018-10-04 |
2020-04-09 |
Inserm (Institut National De La Sante Et De La Recherche Medicale) |
Egfr inhibitors for treating keratodermas
|
|
JP7516029B2
(en)
|
2018-11-16 |
2024-07-16 |
アムジエン・インコーポレーテツド |
Improved synthesis of key intermediates for KRAS G12C inhibitor compounds
|
|
JP7377679B2
(en)
|
2018-11-19 |
2023-11-10 |
アムジエン・インコーポレーテツド |
Combination therapy comprising a KRASG12C inhibitor and one or more additional pharmaceutically active agents for the treatment of cancer
|
|
CA3117222A1
(en)
|
2018-11-19 |
2020-05-28 |
Amgen Inc. |
Kras g12c inhibitors and methods of using the same
|
|
CA3123227A1
(en)
|
2018-12-20 |
2020-06-25 |
Amgen Inc. |
Heteroaryl amides useful as kif18a inhibitors
|
|
WO2020132651A1
(en)
|
2018-12-20 |
2020-06-25 |
Amgen Inc. |
Kif18a inhibitors
|
|
MX2021007157A
(en)
|
2018-12-20 |
2021-08-16 |
Amgen Inc |
Heteroaryl amides useful as kif18a inhibitors.
|
|
PE20211475A1
(en)
|
2018-12-20 |
2021-08-05 |
Amgen Inc |
KIF18A INHIBITORS
|
|
ES2974634T3
(en)
|
2018-12-21 |
2024-06-28 |
Celgene Corp |
Thienopyridine inhibitors of RIPK2
|
|
NL2022471B1
(en)
|
2019-01-29 |
2020-08-18 |
Vationpharma B V |
Solid state forms of oclacitinib
|
|
JP2022522777A
(en)
|
2019-03-01 |
2022-04-20 |
レボリューション メディシンズ インコーポレイテッド |
Bicyclic heteroaryl compounds and their use
|
|
EP3930845A1
(en)
|
2019-03-01 |
2022-01-05 |
Revolution Medicines, Inc. |
Bicyclic heterocyclyl compounds and uses thereof
|
|
EP3738593A1
(en)
|
2019-05-14 |
2020-11-18 |
Amgen, Inc |
Dosing of kras inhibitor for treatment of cancers
|
|
CN114144414B
(en)
|
2019-05-21 |
2025-11-07 |
美国安进公司 |
Solid state form
|
|
US12540129B2
(en)
|
2019-08-02 |
2026-02-03 |
Amgen Inc. |
KIF18A inhibitors
|
|
CA3147272A1
(en)
|
2019-08-02 |
2021-02-11 |
Amgen Inc. |
Kif18a inhibitors
|
|
CN114302880B
(en)
|
2019-08-02 |
2025-07-15 |
美国安进公司 |
KIF18A inhibitors
|
|
WO2021026101A1
(en)
|
2019-08-02 |
2021-02-11 |
Amgen Inc. |
Kif18a inhibitors
|
|
MX2022004656A
(en)
|
2019-10-24 |
2022-05-25 |
Amgen Inc |
PYRIDOPYRIMIDINE DERIVATIVES USEFUL AS INHIBITORS OF KRAS G12C AND KRAS G12D IN THE TREATMENT OF CANCER.
|
|
CN114867735A
(en)
|
2019-11-04 |
2022-08-05 |
锐新医药公司 |
RAS inhibitors
|
|
PE20221277A1
(en)
|
2019-11-04 |
2022-09-05 |
Revolution Medicines Inc |
RAS INHIBITORS
|
|
CN114786777A
(en)
|
2019-11-04 |
2022-07-22 |
锐新医药公司 |
RAS inhibitors
|
|
PE20230249A1
(en)
|
2019-11-08 |
2023-02-07 |
Revolution Medicines Inc |
BICYCLIC HETEROARYL COMPOUNDS AND THEIR USES
|
|
CA3158188A1
(en)
|
2019-11-14 |
2021-05-20 |
Amgen Inc. |
Improved synthesis of kras g12c inhibitor compound
|
|
TW202132271A
(en)
|
2019-11-14 |
2021-09-01 |
美商安進公司 |
Improved synthesis of kras g12c inhibitor compound
|
|
EP4065231A1
(en)
|
2019-11-27 |
2022-10-05 |
Revolution Medicines, Inc. |
Covalent ras inhibitors and uses thereof
|
|
CA3163703A1
(en)
|
2020-01-07 |
2021-07-15 |
Steve Kelsey |
Shp2 inhibitor dosing and methods of treating cancer
|
|
KR20230042600A
(en)
|
2020-06-18 |
2023-03-28 |
레볼루션 메디슨즈, 인크. |
Methods of Delaying, Preventing, and Treating Acquired Resistance to RAS Inhibitors
|
|
CA3187757A1
(en)
|
2020-09-03 |
2022-03-24 |
Ethan AHLER |
Use of sos1 inhibitors to treat malignancies with shp2 mutations
|
|
AU2021345111B2
(en)
|
2020-09-15 |
2025-11-27 |
Revolution Medicines, Inc. |
Indole derivatives as Ras inhibitors in the treatment of cancer
|
|
EP4267250A1
(en)
|
2020-12-22 |
2023-11-01 |
Qilu Regor Therapeutics Inc. |
Sos1 inhibitors and uses thereof
|
|
CR20230558A
(en)
|
2021-05-05 |
2024-01-24 |
Revolution Medicines Inc |
RAS INHIBITORS FOR CANCER TREATMENT
|
|
EP4334324A1
(en)
|
2021-05-05 |
2024-03-13 |
Revolution Medicines, Inc. |
Covalent ras inhibitors and uses thereof
|
|
AR125782A1
(en)
|
2021-05-05 |
2023-08-16 |
Revolution Medicines Inc |
RAS INHIBITORS
|
|
AR127308A1
(en)
|
2021-10-08 |
2024-01-10 |
Revolution Medicines Inc |
RAS INHIBITORS
|
|
WO2023114954A1
(en)
|
2021-12-17 |
2023-06-22 |
Genzyme Corporation |
Pyrazolopyrazine compounds as shp2 inhibitors
|
|
EP4227307A1
(en)
|
2022-02-11 |
2023-08-16 |
Genzyme Corporation |
Pyrazolopyrazine compounds as shp2 inhibitors
|
|
IL314883A
(en)
|
2022-03-07 |
2024-10-01 |
Amgen Inc |
A process for preparing 4-methyl-2-propan-2-yl-pyridine-3-carbonitrile
|
|
WO2023172940A1
(en)
|
2022-03-08 |
2023-09-14 |
Revolution Medicines, Inc. |
Methods for treating immune refractory lung cancer
|
|
AU2023285116A1
(en)
|
2022-06-10 |
2024-12-19 |
Revolution Medicines, Inc. |
Macrocyclic ras inhibitors
|
|
EP4601644A1
(en)
|
2022-10-14 |
2025-08-20 |
Black Diamond Therapeutics, Inc. |
Methods of treating cancers using isoquinoline or 6-aza-quinoline derivatives
|
|
AU2024241633A1
(en)
|
2023-03-30 |
2025-11-06 |
Revolution Medicines, Inc. |
Compositions for inducing ras gtp hydrolysis and uses thereof
|
|
WO2024211663A1
(en)
|
2023-04-07 |
2024-10-10 |
Revolution Medicines, Inc. |
Condensed macrocyclic compounds as ras inhibitors
|
|
EP4688790A1
(en)
|
2023-04-07 |
2026-02-11 |
Revolution Medicines, Inc. |
Macrocyclic ras inhibitors
|
|
WO2024216016A1
(en)
|
2023-04-14 |
2024-10-17 |
Revolution Medicines, Inc. |
Crystalline forms of a ras inhibitor
|
|
AU2024252105A1
(en)
|
2023-04-14 |
2025-10-16 |
Revolution Medicines, Inc. |
Crystalline forms of ras inhibitors, compositions containing the same, and methods of use thereof
|
|
CN121712509A
(en)
|
2023-05-04 |
2026-03-20 |
锐新医药公司 |
Combination therapy for RAS related diseases or conditions
|
|
US20250049810A1
(en)
|
2023-08-07 |
2025-02-13 |
Revolution Medicines, Inc. |
Methods of treating a ras protein-related disease or disorder
|
|
IL327306A
(en)
|
2023-10-12 |
2026-05-01 |
Revolution Medicines Inc |
Macrocyclic ras inhibitors
|
|
WO2025137507A1
(en)
|
2023-12-22 |
2025-06-26 |
Regor Pharmaceuticals, Inc. |
Sos1 inhibitors and uses thereof
|
|
WO2025171296A1
(en)
|
2024-02-09 |
2025-08-14 |
Revolution Medicines, Inc. |
Ras inhibitors
|
|
WO2025240847A1
(en)
|
2024-05-17 |
2025-11-20 |
Revolution Medicines, Inc. |
Ras inhibitors
|
|
WO2025255438A1
(en)
|
2024-06-07 |
2025-12-11 |
Revolution Medicines, Inc. |
Methods of treating a ras protein-related disease or disorder
|
|
WO2025265060A1
(en)
|
2024-06-21 |
2025-12-26 |
Revolution Medicines, Inc. |
Therapeutic compositions and methods for managing treatment-related effects
|
|
WO2026006747A1
(en)
|
2024-06-28 |
2026-01-02 |
Revolution Medicines, Inc. |
Ras inhibitors
|
|
WO2026015790A1
(en)
|
2024-07-12 |
2026-01-15 |
Revolution Medicines, Inc. |
Methods of treating a ras related disease or disorder
|
|
WO2026015801A1
(en)
|
2024-07-12 |
2026-01-15 |
Revolution Medicines, Inc. |
Methods of treating a ras related disease or disorder
|
|
WO2026015825A1
(en)
|
2024-07-12 |
2026-01-15 |
Revolution Medicines, Inc. |
Use of ras inhibitor for treating pancreatic cancer
|
|
WO2026015796A1
(en)
|
2024-07-12 |
2026-01-15 |
Revolution Medicines, Inc. |
Methods of treating a ras related disease or disorder
|
|
WO2026050446A1
(en)
|
2024-08-29 |
2026-03-05 |
Revolution Medicines, Inc. |
Ras inhibitors
|
|
WO2026072904A2
(en)
|
2024-09-26 |
2026-04-02 |
Revolution Medicines, Inc. |
Compositions and methods for treating lung cancer
|
|
WO2026090116A2
(en)
|
2024-10-21 |
2026-04-30 |
Revolution Medicines, Inc. |
Ras inhibitors
|
|
US20260108528A1
(en)
|
2024-10-22 |
2026-04-23 |
Revolution Medicines, Inc. |
Methods of treating a ras protein-related disease or disorder
|
|
WO2026090245A1
(en)
|
2024-10-22 |
2026-04-30 |
Revolution Medicines, Inc. |
Use of ras inhibitors for treating cancer
|